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A Track Record on SHOX: From Basic Research to Complex Models and Therapy

SHOX deficiency is the most frequent genetic growth disorder associated with isolated and syndromic forms of short stature. Caused by mutations in the homeobox gene SHOX, its varied clinical manifestations include isolated short stature, Léri-Weill dyschondrosteosis, and Langer mesomelic dysplasia....

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Detalles Bibliográficos
Autores principales:	Marchini, Antonio, Ogata, Tsutomu, Rappold, Gudrun A.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Endocrine Society 2016
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971310/ https://www.ncbi.nlm.nih.gov/pubmed/27355317 http://dx.doi.org/10.1210/er.2016-1036

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